Details for New Drug Application (NDA): 214803
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The generic ingredient in LIOTHYRONINE SODIUM is liothyronine sodium. There are four drug master file entries for this compound. Twenty suppliers are listed for this compound. Additional details are available on the liothyronine sodium profile page.
Summary for 214803
Tradename: | LIOTHYRONINE SODIUM |
Applicant: | Zydus |
Ingredient: | liothyronine sodium |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Suppliers and Packaging for NDA: 214803
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LIOTHYRONINE SODIUM | liothyronine sodium | TABLET;ORAL | 214803 | ANDA | Northstar Rx LLC | 16714-166 | 16714-166-01 | 100 TABLET in 1 BOTTLE (16714-166-01) |
LIOTHYRONINE SODIUM | liothyronine sodium | TABLET;ORAL | 214803 | ANDA | Northstar Rx LLC | 16714-167 | 16714-167-01 | 100 TABLET in 1 BOTTLE (16714-167-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 0.005MG BASE | ||||
Approval Date: | Jan 22, 2021 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 0.025MG BASE | ||||
Approval Date: | Jan 22, 2021 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 0.05MG BASE | ||||
Approval Date: | Jan 22, 2021 | TE: | AB | RLD: | No |
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